VION ECG Pen - Indonesia BPOM Medical Device Registration
VION ECG Pen is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502220373. The device is manufactured by MD BIOMEDICAL (FOSHAN) CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GLOBAL ENERGY ALKESINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MD BIOMEDICAL (FOSHAN) CO., LTDCountry of Origin
China
Authorized Representative
PT. GLOBAL ENERGY ALKESINDOAR Address
GLOBAL ENERGY ALKESINDO
Registration Date
Nov 11, 2022
Expiry Date
Aug 15, 2027
Product Type
Monitoring Cardiology Equipment
Electrocardiograph.
Non Radiation Electromedics
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